CLASS I Food recall · Reported 16 Nov 2022 · FDA Enforcement Report

Whole Foods Market Dipping Caramel recalled

Whole Foods Market Brand 365 is recalling Whole Foods Market Dipping Caramel, distributed in Colorado, Kansas, Nebraska. The recall was initiated on 27 Oct 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codessell by dates of 10/25/22 - 11/15/22 and available for purchase from 10/4/22 - 10/25/22.

Quantity recalled135 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0147-2023
FDA event ID: 91093
Recalling firm: Whole Foods Market Brand 365, Austin, TX
Classification: Class I
Status: Terminated
Recall initiated: 27 Oct 2022
FDA classified: 10 Nov 2022
Reported: 16 Nov 2022
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Wheat & Gluten
Product category: Candy

Timeline

27 Oct 2022	Recall initiated by company
10 Nov 2022	Classified by FDA	+14 days
16 Nov 2022	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared wheat

Product as listed by the FDA

Whole Foods Market Dipping Caramel, PLU 34888 sold by the pound and packaged in nonflexible plastic containers

Where it was distributed

NE, CO, and KS

Colorado Kansas Nebraska

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Undeclared wheat

Which lots are affected?

sell by dates of 10/25/22 - 11/15/22 and available for purchase from 10/4/22 - 10/25/22.

Where was it sold?

NE, CO, and KS

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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